510(k) K171096 ยท KGE Forceps, Biopsy, Electric
Fujifilm Diathermic Slitter (FlushKnife)
| Applicant | Fujifilm Medical Systems U.S.A, Inc., Wayne NJ, US |
| Decision | Substantially Equivalent, May 9, 2017 |
| Received | Apr 13, 2017 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K171096
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.